Blood pressure and transcranial ultrasound predict moyamoya vasculopathy in Down syndrome
Abstract Aim To evaluate the feasibility of a stepwise, non‐invasive screening framework integrating blood pressure measurement with transcranial Doppler ultrasonography. Method In this prospective single‐site cohort study, 793 individuals with Down syndrome aged 8 to 26 years underwent standardized blood pressure assessment. Comparisons with National Health and Nutrition Examination Survey 2017–2018 were restricted to participants aged 8 years to younger than 18 years and performed using survey‐weighted regression. A smaller cohort of 111 participants underwent repeat blood pressure assessment, awake transcranial Doppler ultrasonography, and confirmatory magnetic resonance imaging/angiography. Results Among 988 screened participants, 793 were enrolled (mean age 16 years 7 months [SD 4 years 6 months]; 414 females, 378 males, and one participant of unknown sex). Mean systolic blood pressure centile was 44.7 in Down syndrome and 42.6 in the comparison cohort (difference 2.07 points, 95% confidence interval [CI] −1.12 to 5.26; p = 0.200). Diastolic blood pressure centile was higher in Down syndrome (difference 12.21 points, 95% CI 8.88–15.53; p < 0.001). Of the 111 participants who completed transcranial Doppler ultrasonography, 10 required repeat acquisition. Higher blood pressure was associated with higher mean middle cerebral artery velocity (75.5 vs 65.7 cm/s; p = 0.006). Imaging identified asymptomatic moyamoya syndrome in four participants. Interpretation A stepwise approach incorporating blood pressure and transcranial Doppler ultrasonography is feasible for cerebrovascular surveillance in Down syndrome. These findings support development of scalable screening strategies and warrant multicenter validation.
Authors
- Benjamin N. Vogel
- Ramón Durazo-Arvizú (ORCID: https://orcid.org/0000-0001-6563-7107)
- Michael S. Rafii (ORCID: https://orcid.org/0000-0003-2640-2094)
- Jonathan Douglas Santoro (ORCID: https://orcid.org/0000-0002-8350-8234)
- Pat Levitt (ORCID: https://orcid.org/0000-0002-9717-1695)
- Elizabeth W. Mayne (ORCID: https://orcid.org/0000-0002-5959-7134)
- Mackenzie Silverman
- Brian G. Skotko (ORCID: https://orcid.org/0000-0002-5232-9882)
- Sarah Lee (ORCID: https://orcid.org/0000-0003-0016-7321)
- Bryan Lei (ORCID: https://orcid.org/0009-0005-1591-968X)
Institutions
- University of Southern California (US)
- Children's Hospital of Los Angeles (US)
- Harvard University (US)
- Palo Alto University (US)
- Massachusetts General Hospital (US)
- Southern California Clinical and Translational Science Institute (US)
- Stanford Medicine (US)
- Southern States University (US)
- Stanford University (US)
Publication Details
- Journal
- Developmental Medicine & Child Neurology
- Published
- 2026-09-29
- DOI
- https://doi.org/10.1111/dmcn.70552
- Primary Topic
- Moyamoya disease diagnosis and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00